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Hydrochloric Acid → 6-Chloro-N-(1H-indol-1-yl)-4-pyrimidinamine

HRID 703458
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인쇄 미리보기

반응식

HRID 703458 반응식
C(O)(C)C.Cl[C:6]1[CH:11]=[C:10]([Cl:12])[N:9]=[CH:8][N:7]=1.Cl.[N:14]1([NH2:23])[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[CH:15]1>O>[Cl:12][C:10]1[N:9]=[CH:8][N:7]=[C:6]([NH:23][N:14]2[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[CH:16]=[CH:15]2)[CH:11]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 3776IsopropanolHCID 709434,6-DichloropyrimidineHCID 6432211-Aminoindole

생성물 1

HCID 151582436-Chloro-N-(1H-indol-1-yl)-4-pyrimidinamine

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
90 °C

실험 절차

To 250 ml isopropanol, was added 4,6-dichloropyrimidine (12 g), 1 ml ethereal -HCl, and 1H-indol-1-amine (15 g). After stirring at 90° C. for seven hours, the mixture was poured into 300 ml iced water, stirred for five minutes, then extracted three times with 200 ml of ethyl acetate. The organic layer was washed with water, then dried (saturated NaCl, anhydrous MgSO4).

후처리

  1. stirringstirred for five minutes
  2. extractionextracted three times with 200 ml of ethyl acetate
  3. washThe organic layer was washed with water
  4. dry with materialdried (saturated NaCl, anhydrous MgSO4)

출처 및 근거

ORD 기록
ord-27f244116b0d493693e72035fba7ed30
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04983608

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